Associated Papers
Rare heterozygous genetic variants of NRXN and NLGN gene families involved in synaptic function and their association with neurodevelopmental disorders.
Gerik-Celebi HB et al.
Developmental Neurobiology, 2024
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia.
Gauthier J et al.
Human Genetics, 2011
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